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Ventilator Settings and Outcomes in Pediatric Patients on ECMO for Severe Respiratory Failure

NCT06899009 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 750

Last updated 2025-03-27

No results posted yet for this study

Summary

This study aims to describe the effects of ECMO initiation on the intensity of ventilation in the first 24 hours after ECMO initiation and to explore associations between changes in ventilation intensity and hospital mortality in critically ill pediatric patients requiring ECMO for respiratory failure, using the 'Extracorporeal Life Support Organization' (ELSO) registry.

Conditions

  • Critical Illness
  • Respiratory Failure (Pediatric Patients)

Sponsors & Collaborators

  • Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

    collaborator OTHER

  • University Medical Center Groningen

    lead OTHER

Principal Investigators

  • Martin CJ Kneyber, MD PhD FCCM · University Medical Center Groningen

  • Marcus J Schultz, MD PhD · Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

  • Frederique Paulus, RN PhD · Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)

Eligibility

Min Age
29 Days
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-01
Primary Completion
2025-03-01
Completion
2025-12-31

Countries

  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06899009 on ClinicalTrials.gov